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Variant (rsID / SNP)

rs3737277

TRIM58

rs3737277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM58. Location: chromosome 1, position 248,023,966. The table records no clinical significance for this variant.

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Reference-table entries

TRIM58Not classified
Variant type
synonymous_variant
Chromosome / position
1:248023966
HGVS
NM_015431.4,c.468C>T,p.Asp156Asp
Allele change
Synonymous_D156D

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.